CANTONI, CLAUDIA

CANTONI, CLAUDIA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 42 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease 1-gen-2011 E. VenturelliC. VillaC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Candidate gene analysis of semaphorins in patients with Alzheimer's disease 1-gen-2010 C. VillaE. VenturelliC. FenoglioM. De RizD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinE. ScarpiniD. Galimberti Article (author) -
Causal frontotemporal de generation mutations : a novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 1-gen-2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. jaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Causal frontotemporal lobar degeneration mutations : a novel mutation in MAPT associated with non-fluent Progressive Aphasia phenotype 1-gen-2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease 1-gen-2011 F. CortiniC. FenoglioE. VenturelliC. VillaM. SerpenteC. CantoniC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Cerebrospinal Fluid Biomarkers in Progranulin Mutations Carriers 1-gen-2011 C. FenoglioF. CortiniM. De RizM. SerpenteC. CantoniN. BresolinE. ScarpiniD. Galimberti + Article (author) -
CHMP5 and BAG1 are protective factors for sporadic frontotemporal lobar degeneration 1-gen-2010 D. GalimbertiC. VillaE. VenturelliC. FenoglioD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinC. MarianiE. Scarpini + Article (author) -
Cognitive decline and extrapyramidal features in a sporadic case of Frontotemporal dementia-parkinsonism caused by a novel progranulin mutation 1-gen-2011 D. GalimbertiF. CortiniC. CantoniE.A. Scarpini + Article (author) -
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis 1-gen-2013 C. FenoglioE. RidolfiC. CantoniM. De RizR. BonsiM. SerpenteC. VillaN. BresolinD. GalimbertiE. Scarpini + Article (author) -
Dimethyl fumarate selectively reduces memory T cells in multiple sclerosis patients 1-gen-2016 Cantoni, ClaudiaGhezzi, LauraPiccio, Laura + Article (author) -
EXPRESSION AND GENETIC ANALYSIS OF MICRORNAS IN MULTIPLE SCLEROSIS AND ITS ANIMAL MODEL EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS 12-feb-2013 C. Cantoni Doctoral Thesis -
Expression and genetic analysis of microRNAs involved in multiple sclerosis 1-mar-2013 E. RidolfiC. FenoglioC. CantoniA. CalviM. De RizA. PietroboniM. SerpenteR. BonsiD. GalimbertiE. Scarpini + Article (author) -
Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with alzheimer's disease 1-gen-2013 Villa, ChiaraRidolfi, ElisaFenoglio, ChiaraSerpente, MariaCantoni, ClaudiaBonsi, RossanaCioffi, SaraMariani, ClaudioScarpini, ElioGalimberti, Daniela + Article (author) -
Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with alzheimer's disease 1-gen-2013 E. RidolfiC. FenoglioL. GhezziM. SerpenteC. CantoniR. BonsiS. CioffiC. MarianiE. ScarpiniD. Galimberti + Article (author) -
Expression profile of miRNAs involved in CD4+ lymphocyte activation and differentiation in patients with multiple sclerosis 1-gen-2010 D. GalimbertiC. FenoglioD. ScalabriniM. SerpenteC. CantoniM. De RizA. PietroboniM. PiolaE. VenturelliC. VillaF. CortiniN. BresolinE. Scarpini + Article (author) -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 1-gen-2012 C. VillaL. GhezziC. FenoglioM. SerpenteC. CantoniE. RidolfiR. BonsiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 1-gen-2012 Villa, ChiaraGhezzi, LauraFenoglio, ChiaraSerpente, MariaCantoni, ClaudiaRidolfi, ElisaBonsi, RossanaMariani, ClaudioBresolin, NereoScarpini, ElioGalimberti, Daniela + Article (author) -
GRN Asp22fs mutation is associated with heterogeneous neurodegenerative clinical phenotypes 1-gen-2010 D. GalimbertiA. PietroboniG. FumagalliL. GhezziC. FenoglioF. CortiniC. CantoniM. SerpenteN. BresolinE. Scarpini + Article (author) -
GRN Asp22fs mutation is associated with highly variable age at onset, clinical phenotype and brain atrophy 1-gen-2010 A. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoP. CortiN. BresolinD. GalimbertiE. Scarpini + Article (author) -
GSK3β genetic variability in patients with Multiple Sclerosis 1-gen-2011 D. GalimbertiD. ScalabriniC. FenoglioM.A. De RizF. CortiniC. VillaM. SerpenteC. CantoniE. RidolfiN. BresolinE.A. Scarpini + Article (author) -